Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,468 positions on this site are linked to Height, out of 2,509,343 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height (baseline)

RAB11FIP3 · rs8046538

See detailed info → Standard

Height

near CARMAL · rs8040851

See detailed info → Standard

Height

near SH3GL3 · rs8039483

See detailed info → Standard

Height (standard GWA)

near ADAMTS5 · rs80171791

See detailed info → Standard

Height (baseline)

PFKP · rs79843289

See detailed info → Standard

Height

SLC41A2 · rs7971575

See detailed info → Standard

Height (baseline)

GUSBP5 · rs79709819

See detailed info → Standard

Height (standard GWA)

LINC02345 · rs79126580

See detailed info → Standard

Height (baseline)

near GSDME · rs78849264

See detailed info → Standard

Height (baseline)

near BNC2 · rs7848057

See detailed info → Standard

Height (baseline)

near CASC20 · rs78223541

See detailed info → Standard

Height

TPD52 · rs7821167

See detailed info → Standard

Height

near RN7SL396P · rs7813113

See detailed info → Standard

Height (standard GWA)

near IGF1 · rs77894464

See detailed info → Standard

Height (baseline)

ASTN1 · rs76850981

See detailed info → Standard

Height (baseline)

SLC9A1 · rs76692181

See detailed info → Standard

Height (baseline)

ADGRG6 · rs76687299

See detailed info → Standard

Height

PRKG1 · rs76442815

See detailed info → Standard

Height (baseline)

near OR51D1 · rs76344430

See detailed info → Standard

Height

near FHIT · rs7625594

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Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.